Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Sneha Saini"'
Autor:
Madhu Sinha, Sneha Saini, Poonam Gupta, Natasha S Gulati, Abhijit Das, Ashok Kumar, Man Mohan Mehndiratta, Chandra Shekhar
Publikováno v:
Indian Journal of Pathology and Microbiology, Vol 61, Iss 3, Pp 461-463 (2018)
Externí odkaz:
https://doaj.org/article/bbda1132af764361a7e335d8a83f4658
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 9, Iss 9, Pp ED03-ED04 (2015)
Otocephaly is a rare malformation characterized by the association of agnathia (agenesis of mandible) or mandibular hypoplasia, melotia (anteromedial malposition of ears), microstomia (small mouth), aglossia or microglossia (absent or rudimentary to
Externí odkaz:
https://doaj.org/article/b042baf763bf427f8ebb4b928e1fa2ca
Autor:
Sneha Saini, Sujata R Kanetkar
Publikováno v:
Journal of Evidence Based Medicine and Healthcare, Vol 3, Iss 103, Pp 5685-5694 (2016)
BACKGROUND Uterine cervix acts as a "gateway" for various infections, which affects cervix, uterus and upper genital tract, thus working under various pathological conditions leading to various lesions of cervix as well as acting as a sentinel for up
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e76780669afa6bdf819a5088a1cebda3
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 9, Iss 9, Pp ED03-ED04 (2015)
Otocephaly is a rare malformation characterized by the association of agnathia (agenesis of mandible) or mandibular hypoplasia, melotia (anteromedial malposition of ears), microstomia (small mouth), aglossia or microglossia (absent or rudimentary ton
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a5475ef07049a5cf791e18df12d8f46
https://europepmc.org/articles/PMC4606241/
https://europepmc.org/articles/PMC4606241/
Publikováno v:
International Journal of Medical Science and Public Health. 5:367
Familial multiple lipomatosis (FML) is a very rare benign condition with the prevalence of 0.002% in general population (1:50,000). It is inherited as an autosomal dominant disease. It is more prevalent in men. It is characterized by multiple, soft-t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a2c2e1ae3ff3f5042538ffa9894fbdf9
https://doi.org/10.5455/ijmsph.2016.1007201547
https://doi.org/10.5455/ijmsph.2016.1007201547